threonine and Hypothyroidism

threonine has been researched along with Hypothyroidism in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Borck, G; Martiné, U; Pohlenz, J; Roth, C; Wildhardt, G	1

Other Studies

1 other study(ies) available for threonine and Hypothyroidism

Article	Year
Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation. The Journal of clinical endocrinology and metabolism, 2003, Volume: 88, Issue:6 Topics: Adolescent; Amino Acid Substitution; Base Sequence; Carrier Proteins; Child; Child, Preschool; Female; Founder Effect; Germany; Haplotypes; Hearing Loss, Sensorineural; Humans; Hypothyroidism; Infant, Newborn; Male; Membrane Transport Proteins; Mutation, Missense; Pedigree; Serine; Sulfate Transporters; Syndrome; Threonine; Turkey	2003

Article

Year

Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.

The Journal of clinical endocrinology and metabolism, 2003, Volume: 88, Issue:6

Topics: Adolescent; Amino Acid Substitution; Base Sequence; Carrier Proteins; Child; Child, Preschool; Female; Founder Effect; Germany; Haplotypes; Hearing Loss, Sensorineural; Humans; Hypothyroidism; Infant, Newborn; Male; Membrane Transport Proteins; Mutation, Missense; Pedigree; Serine; Sulfate Transporters; Syndrome; Threonine; Turkey

2003